WO2011086050A2

WO2011086050A2 - Method for producing aromatic amines in the liquid phase

Info

Publication number: WO2011086050A2
Application number: PCT/EP2011/050233
Authority: WO
Inventors: Wolfgang Lorenz; Bernd Pennemann
Original assignee: Bayer Materialscience Ag
Priority date: 2010-01-14
Filing date: 2011-01-10
Publication date: 2011-07-21
Also published as: CN102712568B; EP2523933A2; RU2561128C9; US20120289745A1; KR20120109555A; JP5805661B2; JP2013517236A; KR101770439B1; WO2011086050A3; RU2561128C2; HUE026176T2; RU2012134506A; US9150493B2; CN102712568A; EP2523933B1

Abstract

The invention relates to a method for producing aromatic amines in the liquid phase by catalytically hydrogenating the corresponding nitroaromatics in at least two reaction chambers connected in sequence, wherein at least one reaction chamber is operated isothermally and at least one reaction chamber connected downstream thereof is operated adiabatically, and preferable embodiments, the sudden adiabatic temperature change is used for controlling the reaction.

Description

Process for the preparation of aromatic amines in the liquid phase

The invention relates to a process for the preparation of aromatic amines in the liquid phase by catalytic hydrogenation of the corresponding nitroaromatics in at least two successive reaction spaces, wherein at least one reaction space is isothermally and at least the reaction space downstream of this adiabatically operated and in preferred

Embodiments of the adiabatic temperature jump is used for the reaction control.

It is known, for example, from EP 0 223 035 AI that aromatic diamines such. B. toluenediamine (TDA, diaminotoluene) can be prepared by catalytic hydrogenation of the corresponding aromatic dinitro compounds. The hydrogenation is carried out with the aid of modified Raney nickel catalysts dispersed in the reaction mixture, which are then separated by filtration or sedimentation and optionally recycled to the process. The focus of this document is on the use of modified Raney nickel catalysts. The use of several series-connected, different (partially isothermal, partially adiabatic) operated reaction spaces is not disclosed there. The hydrogenation reaction described in EP 0 223 035 A1 is very strongly exothermic. Permanent task in the hydrogenation example of dinitrotoluene (DNT) to toluenediamine (TDA) is therefore to dissipate this heat. For example, WO 96/11052 A1 describes a reaction apparatus for carrying out sludge-phase hydrogenations using the heat of reaction for the production of usable steam. There, too, the use of several series-connected, different (partially isothermal, partially adiabatic) operated reaction spaces, not disclosed.

DE-OS-2 044 657 describes a process for the preparation of toluenediamine by hydrogenation of dinitrotoluene at elevated pressure and elevated temperature at one or two reactors connected in series, preferably high pressure tubes, which are equipped with fixed, nickel or ruthenium-containing hydrogenation catalysts. When using two hydrogenation reactors takes place in the first, a turnover of about 90%. It is not explicitly stated whether these reactors should be operated isothermally or adiabatically, except that the same conditions are observed in both reactors. The stated advantage of this process is the elimination of continuous catalyst removal. A disadvantage of this method is that a large amount of the resulting reaction mixture for the purpose of leadership in the circle taken from the product mixture, water removed by distillation and the thus obtained, anhydrous crude hydrogenation must be recycled back into the reaction. No. 3,761,521 describes a process for the hydrogenation of aromatic nitro compounds, in which the hydrogenation is carried out in a stirred container with internal cooling coils. A catalyst separation by means of sedimentation is connected to the reactor. As a result of the differences in density, the reacted reaction mixture circulates from the reactor into the sedimentation tank, where it flows into a catalyst-containing stream and a largely of

Catalyst liberated electricity is decomposed. The former is returned to the reactor, the latter fed to the workup. If the reaction proceeds quickly enough, a reactor / sedimentation tank unit is sufficient for complete reactant conversion. For slower reaction systems, it is recommended that two or more of these systems be connected in series, which requires a lot of equipment. Also in this document, the use of several series-connected, different (partially isothermal, partially adiabatic) operated reaction spaces, not disclosed.

DE 198 44 901 C1 describes a process for the preparation of aromatic amines by the liquid phase process, in which the nitroaromatics are fed via a ring line with holes into the reactor. The loop can also be cooled by an external heat exchanger to eliminate the risk of overheating and thus thermal decomposition of the nitroaromatic. In this method, a particularly good distribution of the nitro aromatic compounds in the reaction mixture should be achieved. Examples of suitable reactors are loop reactors, bubble columns, preferably stirred tanks. Also in this document, the use of several series-connected, different (partially isothermal, partially adiabatic) operated reaction spaces, not disclosed.

A loop reactor is described in EP 0 634 391 A1. Here, a mixture of catalyst and DNT, already formed reaction product and hydrogen mixed by means of an ejector in a container so that the reaction can take place. Essential other elements are a circulation pump, a heat exchanger in the circulation Ström in order to dissipate the heat of reaction and a filter unit for the separation of the product stream and retention of the suspended catalyst. Also in this document, the use of several series-connected, different (partially isothermal, partially adiabatic) operated reaction spaces, not disclosed.

Another method, in which a loop reactor is used, describes WO 00/35852 AI. In this case, a heat exchanger is preferably integrated into the reactor in order to remove the heat of reaction. In addition to the loop reactor, an external circulation is described, wherein preferably in the lower region of the loop reactor reaction mixture is withdrawn and fed by means of a conveying member to the upper region of the reactor. This outer one Circuit may contain an additional heat exchanger and may serve for product discharge with retention of the catalyst by means of, for example gravity separator, cross-flow filter or centrifuge. The reaction procedure is described as highly isothermal. In addition, to complete the reaction in the outer circuit may be a post-reactor. The possible type of this secondary reactor is generally specified as the same or the same as the main reactor or as a stirred tank or as a flow tube. It is not discussed how a required post-reaction is detected or carried out under the reaction conditions. WO 00/35852 teaches that the reaction of dinitrotoluene to toluenediamine takes place virtually quantitatively in the main reactor and the external loop stream contains essentially pure toluenediamine, water and optionally solvent and catalyst. Toluene diamine is taken from the external loop flow and fed to further workup. The use of an adiabatically operated postreactor and the reaction control by monitoring the adiabatic temperature jump is not taught in WO 00/35852.

However, the possibility of the occurrence of unreacted nitro compounds in a reaction system as in WO 00/35852 is described in DE 102 06 214 AI. DE 102 06 214 A1 teaches that the reaction of the nitroaromatics takes place more completely by changing the task of the starting materials (flow direction of at least part of the hydrogen and / or of the nitroaromatic in the liquid reaction mixture). This is especially true for the hydrogenation of DNT. Also in the process in DE 102 06 214 Al, the heat of reaction is removed at the place of formation. The use of an adiabatically operated postreactor and the reaction control by monitoring the adiabatic temperature jump is not taught in this document.

A disadvantage of all processes is that the reaction mixture obtained in addition to the target product of the aromatic amines, the by-product water and from the known side reactions such as nuclear hydrogenations or hydrogenolytic cleavages resulting compounds or high molecular weight, tarry products also used as reactants nitroaromatics or intermediates of the reaction such as nitro may have aromatics. It is known that these compounds, especially in the presence of amines and at elevated temperature are less stable and can decompose explosively. It must therefore be ensured that the implementation is complete. Usually, therefore, the reaction is monitored. This can be done, for example, by gas chromatographic analysis of the product stream, as described in WO 03/066571 Al. Another approach is by monitoring the mass flow entering the reaction as described in DE 102 06 214 AI. DE 10 2005 008 613 A1 describes a process for preparing aromatic amines in which the contents of nitro and nitroso compounds in the reaction product are determined by UV-VIS absorption. DE 10 2005 008 613 A1 teaches that in the catalytic hydrogenation of nitro aromatics, the catalysts are deactivated over time. The lower the activity of the catalysts, the lower the proportion of starting materials converted to amines, so that the

Reactor remaining proportion of unreacted nitroaromatic increases. Therefore, it is necessary to monitor the catalyst activity, particularly to supply the reactor with a sufficient amount of unconsumed catalyst. The method should also be used for dosing of nitroaromatic and fresh catalyst to the reactor system. A disadvantage of this method is that the spectra of TDA / water mixtures with and without nitro / nitroso compounds differ only slightly, which requires complex calibrations. In addition, linings on the measuring cells change the measuring signal, so that the calibration must be checked regularly. Also gas bubbles or catalyst particles interfere with the measurement, so that a complex sample preparation is required, which, in addition to the loss of time between occurrence and detection of the effect, not only high costs, but also low reliability of the overall arrangement causes.

WO 02/062729 A2 deals with the improvement of mass transfer processes in heterogeneously catalyzed hydrogenation reactions, such as, for example, the preparation of aromatic amines from the corresponding nitro compounds. By a certain inert gas content in the hydrogenation hydrogen, a higher hydrogen saturation of the liquid phase in the reactor should be achieved, which should prevent an increased aging of the hydrogenation catalyst and an insufficient selectivity of the reaction. The goal of this publication, it is ultimately to ensure the fullest possible implementation of the nitro compound to the amine in the hydrogenation reactor. It does not cover the control of the hydrogenation quality, ie the effect of catalyst aging or insufficient selectivity, and how to deal with such situations. The basic idea in the above-mentioned processes is either to dissipate the heat of reaction by means of heat exchangers at the place of formation or to take them up in a sufficiently large product stream and to remove them at another location by means of heat exchangers in such a way that inadmissibly high temperatures are avoided. The aim of the methods mentioned is therefore to increase regularly the flow of heat exchangers used for the removal of heat and the mixing of the apparatuses used for the reaction in such a way that the temperature differences in the reaction space are as low as possible. For a rapid hydrogenation is also essential to the presence of sufficient levels of hydrogen in the reaction space, which requires the entry of gas bubbles in the reaction space and can be achieved, for example by means of gassing, Kreisgasverdichter or loop reactors. This fumigation also leads to an intensive mixing of the reaction space. It is obvious that by these measures the residence time distribution approximates that of an ideally mixed stirred tank, which favors the appearance of educts in the product stream and which therefore is undesirable as stated above. With the use of cascaded isothermal and adiabatically operated reactors with

Fixed bed catalysts in the gas phase ydrie ng of nitroaromatics are concerned with EP 1 524 259 A1 (preferably nitrobenzene as starting material) and GB 1 452 466 (excluding nitrobenzene as starting material). The problem of explosion protection in gas phase hydrogenations is far from being as stated above for liquid-phase hydrogenations (in particular of nitroaromatics). Thus, the possibility of the temperature jump in an adiabatic operated

Reaction space for monitoring the conversion of nitro or nitrosoaromatics in any of the two writings taught. EP 1 524 259 A1 only deals with extending the operating time of an isothermally operated main reactor (tube bundle reactor) through a downstream, adiabatically operated reactor with monolithic catalyst when diluting the catalyst bed to dampen the reactivity of the main reactor (page 4, line 32) - 33 and Z. 40). The use of monoliths is essential to the invention in order to avoid unacceptably high differential pressures. Finally, in GB 1 452 466, the combination of isothermal and adiabatic driving provides better temperature control (page 3, lines 86-94). As advantageous in this method, the increase in the space-time yield and the service life are called. The process engineering challenges are completely different in gas phase hydrogenation than in liquid phase hydrogenation, so that the two processes are hardly or not at all comparable.

The object of the present invention is therefore to provide a process for the hydrogenation of nitroaromatics, in particular dinitroaromatics, to the corresponding aromatic amines, in particular diamines, in the liquid phase, in which the residual content of nitroaromatics (ie starting nitroaromatics and in the case of Dimtroverbindungen as Eduke additionally Intermediate occurring aromatic mononitro monoamine compounds) and possibly occurring as intermediates nitrosoaromatics (ie all conceivable, containing at least one nitroso group intermediates) is minimized in the crude product mixture obtained and that a simple and reliable monitoring of the course of the reaction (completeness of the reaction of the nitroaromatic the aromatic amines).

The invention thus relates to a process for the preparation of aromatic amines of the formula

in which R 1 and R 2 independently of one another denote hydrogen, methyl or ethyl, where R 1 can additionally denote NH ₂ , by hydrogenation in the presence of a catalyst of nitroaromatics of the formula

in which R ₂ and R ₃ independently of one another denote hydrogen, methyl or ethyl, where R ₃ may additionally denote NO ₂ , in the liquid phase in at least two cascaded reaction chambers arranged in one or more reactors, at least one reaction space being isothermal and at least one thereof downstream reaction space is operated adiabatically.

The hydrogenation of the nitroaromatic to the corresponding amine takes place with hydrogen or mixtures of hydrogen and inert gases as hydrogenation reagent. All catalysts which are customary for catalytic hydrogenations are suitable as catalysts. Preference is given to using catalysts which contain noble metals such as Pt, Pd, Rh, Ru or non-ferrous metals such as Ni, Co or Cu or mixtures thereof. Particular preference is given to using catalysts which comprise Pt, Pd, Ni or Cu as suspension in water. In the case of noble metal catalysts, these are applied to carriers such as activated carbon, S1O ₂ or Al ₂ O ₃ , in the case of Ni catalysts may also

Raney-Ni can be used. The concentration of catalyst in the reaction space is preferably between 0.01% by mass and <20% by mass, preferably between 0.5% by mass and 10% by mass, based on the total mass of the reaction mixture in the reaction space. If mixtures of hydrogen and inert gases are used, preferred inert gases are ammonia, noble gases and / or nitrogen. Hydrogen or the mixture of hydrogen and inert gases is preferably fed in such a way that a constant pressure is established in the reaction space, ie with increasing reaction progress (and thus hydrogen consumption) the supply of fresh hydrogenation reagent is increased. In the case of using a mixture of hydrogen and inert gases as the hydrogenation reagent, the ratio of hydrogen and inert gas in the supplied hydrogenation reagent is preferably increased successively so as not to allow the reactor contents to become depleted of hydrogen. The reaction space is understood to mean the space in which the conditions for a reaction in the liquid phase of nitroaromatic (or intermediates) with hydrogen are given to the desired aromatic amine. The reaction space is located in a technical device for carrying out chemical reactions, the reactor. Depending on the design, the reaction space and the reactor may also be identical (eg in bubble column reactors). Of the

Reaction space may also comprise only part of the reactor. If, for example, a liquid phase is present only in the lower region of a reactor, the gas phase above no longer forms a reaction space according to the invention, despite the fact that, as a result of the vapor pressure of the nitroaromatic, a fraction of the nitroaromatic which enters the gas phase may occur and react there. A reactor may also contain several reaction spaces. The reaction spaces can be located in one or in different reactors. Preferred reactors for the process according to the invention are stirred vessels, loop reactors, flow tubes, bubble column reactors or jet reactors.

The reaction spaces are cascaded in the process of the invention, d. H. the product mixture from a reaction space is introduced into the following reaction space as Edukt- mixture. It is possible, but not absolutely necessary, to additionally introduce fresh hydrogen or a mixture of hydrogen and inert gases and optionally fresh catalyst into the downstream reaction spaces. In the process according to the invention, the fresh nitroaromatic is introduced only into a reaction space; this is referred to as the first in the direction of flow of the nitroaromatic and preferably operated isothermally. All subsequent ones

Reaction spaces are charged only with nitroaromatics, which was not reacted in the respective previous reaction space. Accordingly, at full conversion in the direction of flow of the nitroaromatic first reaction space, the following are not charged at all with nitroaromatics.

It is also conceivable to connect more than two reaction chambers in series, that is to say, for example, cascades such as "isothermal adiabatic - adiabatic" (cf., FIG. 4), "isothermal - isothermal - adiabatic - adiabatic" or other combinations. Preferably, a maximum of 10 reaction spaces are connected in series, particularly preferably at most 5, very preferably at most 3, exceptionally very preferably at most 2. The first reaction space of a cascade in the inflow direction of the nitroaromatic is preferably isothermic and the last reaction space of this cascade is operated adiabatically. The invention is explained in more detail below with reference to the embodiment with two successive reaction spaces. It is easy for those skilled in the art to transfer the information to systems with more than two reaction spaces, if necessary. Isothermal in the context of the present invention means that at least the major part of the heat released by the reaction is removed by technical devices. Preferably, the heat of reaction is completely removed by technical devices. Such devices may be: shell and tube heat exchangers, tube coils, plate heat exchangers, field tubes, U-tube heat exchangers. These devices are preferably mounted in the isothermally operated reaction space. Alternatively, they may also be outside of the isothermally operated reaction space, if a sufficient isotherm (ie at most a negligible temperature rise) in the reaction space is ensured by sufficiently large circulation flows. Accordingly, adiabatic in the context of the present invention means that the heat of reaction in the adiabatically operated reaction space is not dissipated by technical devices. In adiabatic operation, the reaction space can be isolated in a special way against heat loss. When heat losses are negligible, the reaction enthalpy is quantitatively reflected in the temperature difference between inlet and outlet flows. Reaction in the liquid phase means that the reaction takes place at such physical

Conditions, in particular of pressure and temperature, is carried out, in which the nitro-aromatics, intermediates and the aromatic amine are liquid. Preference is given to absolute pressures between 6 bar and 101 bar, preferably between 10 bar and 30 bar and temperatures between 50 ° C and 250 ° C, preferably between 100 ° C and 200 ° C, more preferably 120 ° C and 195 ° C, in complied with all reaction rooms. Within these ranges, pressure and temperature may be different in each reaction space.

The pressure in the adiabatically operated reaction space is preferably equal to the pressure in the preceding isothermally operated reaction space. The pressure is preferably measured in the head region of the reactor. In certain embodiments of the method according to the invention, therefore, the measuring point for the pressure is outside the actual reaction space (for example in the gas phase above the liquid phase representing the reaction space). This pressure thus measured is not necessarily identical to the pressure in the reaction space itself, but in any case characteristic of it, so that it represents a suitable reference point for relative comparisons between pressures in different reaction spaces. The pressure in the adiabatically operated reaction space can also be slightly below the pressure in the isothermally operated reaction space. However, if the pressure in the adiabatically operated reaction chamber is lowered too sharply compared to the pressure in the isothermally operated reaction space, a flash evaporation of the reaction mixture occurs in the feed of the adiabatically operated reaction space, which leads to a clear Reduction of the proportion of dissolved and / or dispersed hydrogen in the liquid phase leads. For the process according to the invention, therefore, the ratio of the pressure in any adiabatically operated reaction space to the pressure in the respective preceding isothermally operated reaction space is greater than 0.5, preferably greater than 0.7, and particularly preferably greater than 0.9.

Preferably, the temperature set by means of suitable devices for heat dissipation in the isothermally operated reaction chamber corresponds to the inlet temperature of the adjoining adiabatic reaction space downstream of this.

Optionally inert solvents can be used under the reaction conditions, such as. As alcohols such as methanol, propanol, isopropanol or ethers such as dixoane, tetrahydrofuran. In order to increase the economy of the process, a low solvent concentration is generally advantageous; Usually this will be between 1 mass% and <50 mass%, preferably between 20 mass% and <35 mass%, based on the total mass of the liquid phase.

The conversion of nitroaromatics and optionally of the nitrosoaromatics occurring as intermediates in the first reaction space in the direction of flow of the nitroaromatic is preferably too

Start of hydrogenation, when the catalyst is still fresh and highly active, 100%. As the catalyst deactivation proceeds, the conversion in this reaction space will continue to decline, unless countermeasures are taken. The unreacted proportions of nitro and optionally nitrosoaromatic are preferably further reacted in the process according to the invention in the adiabatically operated reaction space, particularly preferably completely.

The inventive method is particularly suitable for the hydrogenation of DNT (in formula II: R2 = methyl and R3 = N0 ₂ ) to TDA (in formula I: Rl = NH ₂ and R2 = methyl). In the industrial process, all isomers occur, but mainly 2,4-TDA and 2,6-TDA.

The process according to the invention is preferably carried out continuously. However, a discontinuous driving style is not excluded.

In a preferred embodiment of the present invention, an adiabatically operated reaction chamber is followed by an isothermally operated reaction space, wherein the product mixture containing suspended catalyst obtained from the isothermally operated reaction space is introduced into the adiabatically operated reaction space and, after further, preferably complete, conversion into two streams, one of which is largely freed from catalyst and fed to further workup. For the separation of catalyst are heavy force separation, for example Settier and filtration, for example, cross-flow filter. The catalyst thus obtained can, if appropriate after work-up processes, be recycled to the isothermally operated reaction space. Optionally, even fresh catalyst can be supplied. The other, catalyst-containing stream is returned to the isothermally operated reaction space. The separation of water of reaction from this recycled

Electricity is possible but not preferred.

The transport of the reaction mixture from the isothermally operated reaction space into the adiabatically operated reaction space can take place in various ways in this embodiment, for example by pumping or under the influence of gravity by means of overflow or density differences. The same applies to the return transport of the catalyst-containing stream.

In a further embodiment, a reactor is divided by suitable flow guidance into two reaction spaces (see FIG. 4). The first reaction space in the direction of flow of the nitroaromatic is provided with a device for heat removal ("isothermal reaction space") and the second not ("adiabatic reaction space"). The hydrogen or the mixture of hydrogen and inert gases is entered only in the "isothermal reaction space".

The series connection according to the invention of an isothermally operated and an adiabatically operated reaction space makes use of the advantages of both process methods and thus stands out in a particularly advantageous manner from the prior art. Thus, the major part of the conversion (preferably more than 95%, more preferably more than 98%, very preferably more than 99%) of Ausgangsmtroaromat and any intermediates occurring in the isothermally operated reaction chamber under mild conditions, the highest level of safety guarantee. The implementation of the remaining nitroaromatic and any remaining intermediates under adiabatic conditions on the one hand makes use of the fact that the higher temperatures (no heat dissipation!) In the adiabatically operated reaction space higher conversions are possible (which, since only a small portion of Ausgangsnitroaromaten and all possibly occurring intermediates must be implemented safely) and on the other hand also offers the additional advantage of easy monitoring of the course of the reaction, in particular the completeness of the hydrogenation reaction of nitroaromatics to aromatic amine, by controlling a suitable carried out for the adiabatically operated reaction space Part of the hydrogenation characteristic, characteristic. Suitable parameters may be, inter alia: color, temperature, the concentration of compounds containing nitro and nitroso groups, determined by chemical analysis, preferably by gas chromatography, or by spectroscopic analysis, preferably by UV-VIS spectroscopy. Become several Adiabatically operated reaction chambers used, so the control of this appropriate parameter for one, several or all adiabatically operated reaction chambers can be performed. In a cascade of more than two reaction spaces, at least the last reaction space is preferably operated adiabatically and the characteristic parameter is controlled at least for this latter. In principle, also different parameters can be controlled, for example temperature and color.

Preference is given to determining a critical value for each parameter by preliminary tests, for example in the case of temperature a critical temperature which can not be exceeded, as will be explained in more detail below. Upon reaching or exceeding this previously defined critical value of this parameter, then (at least) one process parameter can be changed so that this parameter again drops below the critical value, as will be explained in detail below. The critical value for the concentration of compounds containing nitro and nitroso groups is highly dependent on the specific boundary conditions of a production plant (eg temperature, pressure, type of nitroaromatic to be hydrogenated and catalyst used). It may, for example, preferably at values of less than 5.0% by mass, particularly preferably less than 2.0% by mass and very particularly preferably less than 0.5% by mass, in each case based on the total mass of the product outlet stream of the adiabat operated reaction space lie.

The inventive method allows in preferred embodiments, the determination of an at least qualitative, preferably quantitative relationship between certain parameters and the content of nitro / Nitrosoaromaten in entering and / or leaving the adiabatically operated reaction space by testing or by engineering calculations. During actual production, by controlling one or more of these parameters, it can then be determined when at least one process parameter needs to be changed in order to increase sales again. In this context, in particular the temperature is the parameter of choice, as will be explained in more detail below. The characteristic color eludes a simple quantitative description. However, experienced plant operators can already draw conclusions on the course of the reaction on the basis of color observations (for example in sampling points located in the product outlet from the adiabatic reaction space).

For the purpose of quantifying the relationship between certain suitable parameters and the content of nitro / nitrosoaromatics entering and / or leaving the adiabatically operated reaction space, it may be appropriate in certain cases to use one calibration curve, possibly several calibration curves for different ranges of Pressure and temperature, create. Is used as a reference value of the content of nitro / Nitrosoaromaten in the entry in Depending on the performance of the adiabatically operated reaction space, at least one process parameter is changed in good time to ensure that the amount of nitro / nitroso aromatic compounds entering the adiabatically operated reaction space can be converted as completely as possible. For example, the temperature tadiabat measured in the adiabatically operated reaction space or in the product outlet from the adiabatically operated reaction space can be a suitable parameter. The critical value of the parameter tadiabate, tadiabat crit, is preferably between 200 ° C and 250 ° C, depending on the exact other process conditions and the type of nitroaromatic to be hydrogenated. The process according to the invention makes it possible to monitor the course of the reaction (completeness of the hydrogenation reaction of nitroaromatics to aromatic amine), in particular also by measuring a temperature difference ATadiabat (adiabatic temperature jump) between at least one of the adiabatically operated reaction spaces and the preceding isothermal reaction space. This type of reaction control, which is not possible with purely isothermal reaction control, is particularly preferred.

The temperature difference ATadiabat is preferably determined by measuring the temperature tadiabate in the product outlet from the respective adiabatically operated reaction space or in the respective adiabatically operated reaction _space itself and by measuring the temperature T isoth in the respective preceding isothermally operated reaction space or in the entry into the respective adiabatically operated reaction space and Subsequent difference formation according to

ATadiabat Tadiabat Ti _so thermo-

If the temperature in the product outlet from the adiabatically operated reaction space is used for the determination of tadiabat, the measurement does not necessarily have to take place immediately after

Leaving the adiabatically operated reaction space done. The temperature measuring point can also be, for example, behind the catalyst separation. It merely has to be ensured that the measuring point allows reliable information about the heat development in the adiabatically operated reaction space. If a cascade of reaction spaces contains more than two adiabatically operated, then, although not preferred, several such adiabatic temperature jumps can be measured. For example. can in a reaction chamber cascade of the type "isothermal (1) - adiabatic (1) - isothermal (2) - adiabatic (2)" two temperature differences, AT adiabatic (1) = tadiabate (1) - T _isothermal (1) and AT adiabatic (2) = Tadiabate (2) - tisotherm (2) If two adiabatically operated reaction spaces are connected in series, ie "isothermal - adiabatic (1) - adiabatic (2)", the temperature difference tadiabate (2) - Ti is preferred _sothe rm. In this case, the "preceding" isothermally operated reaction space is not the immediately preceding reaction space (which is also operated adiabatically.) The temperature measurement is carried out by means of devices known to the person skilled in the art, such as thermocouples or resistance, semiconductor or infrared thermometers Determination of Τ _ί8θύιε πη in an isothermally operated reaction space is, for example, in a stirred reactor, the environment in the vicinity of the stirrer or preferably the area of the reactor wall surrounding the stirrer A temperature thus measured within the isothermally operated reaction chamber is i A suitable site for the determination of tadiabate in the adiabatically operated reaction space is near the reactor wall in the region of the exit from the adiabatically operated reaction space ture in the product outlet from the adiabatically operated reaction space is generally identical to the average temperature reached as a result of the heat development in this adiabatically operated reaction space (= adiabatic transition temperature; to distinguish from the adiabatic temperature jump ATadiabat) - It is essential that the measuring points are chosen such that they are representative of the mean adiabatic transition temperature in the adiabatically operated reaction space and for the mean temperature in the isothermally operated reaction space. Preferably, a quantitative relationship between ATadiabat and the

Content of the sum of nitroaromatics and possibly of the nitrosoaromatics occurring as intermediates in the product outlet of the adiabatically operated reaction space determined. For example, a calibration curve can be determined by a few tests, which is a function

ATadiabat = ATadiabat (Cl {nitro / nitrosoaromatic, exiting adiabatic}); C = concentration, represented in mass%. Of course, ATadiabate also depends on the individual temperatures and pressures. Also preferred is a maximum permissible temperature difference, hereinafter referred to as ATadiabat, _max . designated, determined. This corresponds to that temperature difference which corresponds to a content of the sum of nitroaromatics and, if appropriate, of the nitrosoaromatics occurring as intermediates in the product outlet of the adiabatically operated reaction chamber, which is just acceptable under quality and explosion protection aspects. Such a maximum tolerable content is preferably values up to 5.0% by mass, more preferably up to 2.0% by mass and most preferably up to 0.5% by mass, in each case based on the total mass of the product outlet stream. Preferably, a value of ATadiabat is further determined, which is so far below ATadiabat, max. is that by changing at least one process parameter the achievement of ATadiabat, max. can be prevented in good time. This value is the critical value of

Characteristic ATadiabat and is called ATadiabat, crit.

The determination of ATadiabat, max and ATadiabat, crit can be done on the one hand by experiments in which a sufficient amount of starting material is in the feed to the adiabatically operated reaction chamber or on the other hand by engineering calculations on the temperature profile in the adiabatically operated reaction space. The measured in normal production operation then each temperature difference ATadiabat is with the maximum temperature difference ATadiabat, max. and / or ATadiabat, crit.

If ATadiabat ⁼ 0, if heat losses can be neglected, the reaction takes place completely in the isothermally operated reaction space, ie the conversion of nitroaromatics and possibly of the nitrosoaromatics occurring as intermediates in the isothermally operated reaction space is 100%. An AT adiabatic <0 indicates heat losses due to imperfect isolation. An AT adiabatic> 0 indicates incomplete conversion in the isothermally operated reaction space.

The value of ATadiabat in a particular case requiring the modification of at least one process parameter (i.e., when ATadiabate becomes ATadiabat, Crit.) Depends on many factors. The range within which AT adiabatic becomes AT adiabatic, crit., May generally assume values between -10K and +8K, preferably between -8K and +5K, more preferably between -5K and +3K.

If a production plant is very well insulated so that at full conversion in the isothermally operated reaction space, ATadiabat = 0, a value of ATadiabat <0 reliably indicates that no hydrogenation reaction takes place in the adiabatically operated reaction space. In such a case are

Values of ATadiabat that are only slightly greater than zero are generally not critical. In Particularly preferred embodiments, the critical value VOn ATgdiabat. (ATgdiabat, crit.) +3 K.

On the other hand, in the case of a poorly isolated production plant, a value of

Falsely pretend that no reaction takes place in the adiabatic reaction space. In such a case, even at values of ΔΤ ^^ ^ Ο, at least one process parameter may need to be changed. So it is useful in particularly preferred embodiments, already at values of

is -5 K) to change at least one process parameter.

If the control of one or more of the abovementioned suitable part of the hydrogenation which is characteristic for the part of the hydrogenation carried out in the adiabatic reaction space, indicates characteristic values for incomplete conversion in the isothermally operated reaction space, there are several possibilities: a) Continuing the reaction under constant conditions up to Reaching a maximum permissible value of the respective parameter (eg at

_max ) the reaction is aborted (triggering of an alarm and / or automatic shutdown). b) changing at least one process parameter so that the appropriate characteristic decreases. Possible changes are, for example: ba) supply of fresh catalyst; bb) increasing the recycled amount of used catalyst; bc) Gradual reduction of the amount of fresh nitroaromatics fed in; bd) increasing the pressure in at least one of the reaction spaces; be) raising the temperature in at least one of the reaction spaces.

It is preferable not to allow the amount of hydrogen dissolved and dispersed in the feed to the adiabatically operated space to drop as much as possible. By dispersed hydrogen is meant gas entrained in gas bubbles. In the process, it is preferable to add enough hydrogen to the reaction space so that a constant pressure is established; and a small gas stream is taken from the gas phase of the isothermal and adiabatic reaction space and, if appropriate, analyzed for its composition (for example by gas chromatography). graphy). In this way, converted hydrogen is added and it will be discharged accumulating inert gases or gaseous reaction products.

It is essential for the process according to the invention that the hydrogenation reaction in the adiabatically operated reaction space can even be completed. This requires that the amount of dispersed and dissolved hydrogen in the feed to the adiabatically operated reaction space exceed the amount required for the reaction. It is known to the person skilled in the art that the amount of dissolved hydrogen depends on the composition of the reaction mixture, the pressure and the temperature in the isothermally operated reaction space and the composition of the gas phase in this reaction space. For the content of dispersed and dissolved hydrogen, inter alia the fumigation in the reaction space and the relative velocity of the liquid and gas phases are of importance. The composition of the gas phase is characterized by the partial pressures of the components in the liquid phase and their interaction with each other, the formation of gaseous by-products such. As ammonia and the presence of impurities in the supplied hydrogen and their accumulation in the reactor determined. It is furthermore essential that the liquid phase in the adiabatically operated reaction space has a residence time which is sufficiently long to allow residual conversion. For the process according to the invention, the adiabatically operated reaction space has a residence time of the liquid phase which is at least 10% of the residence time of the liquid phase of the isothermally operated reaction space, at least 20% and at most 300% being preferred. The process of the invention is particularly well suited in the event of an expected gradual and slow reduction in reaction rate from a high reaction rate state, typically but not exclusively caused by progressive catalyst deactivation. The adiabatically operated reaction space downstream of the isothermally operated reaction space allows higher conversions due to the higher temperatures (no heat removal!), Whereby the catalyst deactivation is at least partially compensated again. Of course, the other prerequisite for further reaction progress, such as sufficient hydrogen and catalyst, must be given. Optionally, hydrogen and catalyst can therefore be metered separately into the adiabatically operated reaction space. The workup of the product mixture freed from the catalyst initially comprises the separation of the reaction water formed during the hydrogenation of the nitro groups by distillative separation known to the person skilled in the art. This is followed by the separation of by-products (eg partially or completely ring-hydrogenated and / or deaminated and / or demethylated nitroaromatic compounds, Ammonia (deamination product), optionally reaction products of the solvent (if this is not completely inert), azoxy, etc.). The desired aromatic amines are separated from higher-boiling impurities (residue) and, if necessary, separated into their isomers. These separation operations are preferably carried out by the skilled person known distillation.

FIG. 1 shows an embodiment of the invention. Stream 1 denotes the educt mixture to be hydrogenated (nitroaromatic, and optionally inert solvent). Preferably, nitroaromatic and catalyst are added separately; the exact location of the catalyst addition (not shown in FIG. 1) is not essential to the invention. Stream 2 denotes hydrogen, A the reactor with isothermally operated reaction space, stream 3 the reaction mixture entering reactor B with adiabatically operated reaction space. Stream 4 designates the reacted mixture entering the filtration C (here cross-flow filter), stream 5 is used to return the thickened mixture of reaction product and catalyst to the reactor, stream 6 designates the reaction product fed to the work-up and stream 7 the discharge of Inert gases serving gas stream. The pump D serves to maintain the circulation. The monitoring of the completeness of the reaction can be done for example by measuring the temperature difference ATadiabat between the streams 3 and 5, 3 and 4 or 3 and 6.

Figure 2 illustrates an embodiment in which the functions of the reactor B with adiabatically operated reaction space and the catalyst separation C in an apparatus E is summarized.

FIG. 3 describes an embodiment of the invention in which the pump D can be dispensed with and the recirculation of the thickened reaction mixture from the apparatus E with adiabatically operated reaction space with apparatus for catalyst separation (in this case gravitational separator) into the reactor A with isothermally operated reaction space by means of the density - distinguished the liquid phases.

Figure 4 describes an embodiment in which the reactor A ', which contains an isothermally operated reaction space AI, additionally contains an adiabatically operated reaction space A2 by means of suitable flow guidance. The separation of the two reaction spaces can be done by internals (G), for example by sieve plates, baffles, heat exchangers or the like. The flow in the lower region of the reactor is turbulent and increasingly uniform towards the top, in particular behind G. In this arrangement, the total adiabatically operated reaction space consists of two individual adiabatically operated reaction spaces, viz from the liquid reactor contents of the apparatus E and a part of the volume of the intensely fumigated reactor A ', namely A2. This arrangement has the advantage of a particularly high gas supply in the first adiabatically operated reaction space (A2) and thus enables the conversion of a larger proportion of nitroaromatics (eg dinitrotoluene) and thus also a larger adiabatic temperature difference ΔΤ ^^ between E and AI, which the measuring task further facilitated. The gas bubbles introduced into AI move through the adiabatically operated reaction space A2, so that much more nitro and nitroso groups can be hydrogenated than in E alone. ΔΤ ^^ can be determined in this arrangement by measuring the temperature in the vicinity of the stirrer AI and the temperature of the exiting from apparatus E product stream. 5

FIG. 5 shows a quantitative relationship between the adiabatic temperature jump of the hydrogenation of DNT and the concentration of nitrotoluidine present at least in the inlet stream of the adiabatically operated reaction space (see Example 2).

Examples

Example 1 (according to the invention)

A test arrangement according to FIG. 1 consisting of a reactor A with isothermally operated reaction space with 1 l reaction volume and internal heat exchanger, a reactor B with adiabatically operated reaction space with a volume of 1 l and a device for

Catalyst separation consisting of a circulating pump (D) with frit (C) is dinitrotoluene (isomeric mixture of 2,4-, 2,6-, 2,3-, 3,4-, 2,5-DNT) hydrogenated. The recycle stream 5 of 2.5 1 / h promotes the separated in apparatus C from the stream 6 catalyst in the reactor A. The hydrogen stream 2 is adjusted so that in each case an absolute pressure of 25 bar results in both reaction spaces. Approximately 4 vol .-% of the supplied hydrogen are discharged for the purpose of discharge of impurities and gaseous by-products via stream 7. The reacted mixture stream 6 is analyzed by gas chromatography. Cooling water is passed through the heat exchanger, the amount of which is adjusted so that a temperature in the reaction space of A of 120 ° C is established. A total of 40 g of Raney Ni suspended in water are added as the hydrogenation catalyst. Temperatures in stream 4 and in the reaction space near the

Stirrer are measured, their difference calculated and recorded. The reaction is started by supplying a stream of 400 g / h of dinitrotoluene (1). A temperature difference ATadiabat = T (4) - T (A, stirrer) = -1 K is measured (i.e., no reaction takes place in B), while in stream 6 no nitroaromatics can be determined by gas chromatography. The reaction is carried out under otherwise constant conditions until the temperature difference ATadiabat has risen to +8 K (i.e., in A the DNT is no longer completely reacted). This is reached after 360 hours. Then the reaction is stopped and found a content of 3.8% by mass nitrotoluidines in stream 6.

Example 2 (According to the Invention) Based on the heat of reaction for the hydrogenation reaction and the heat capacity of the reaction

Example 1 of the mixture shown in Figure 5 between ATadiabat = T (4) - T (A, stirrer) and found in the stream 3 to the adiabatic reaction space concentration found on the intermediate nitrotoluidine (C _N T;, indicated in mass% on the total mass of the stream 3) determined. C _N T is the z esikonzentration of nitrotoluidine under the assumption of perfect thermal insulation. The relationship shown in Figure 5 is further based on the assumption that in the adiabatically operated reaction space is always sufficient hydrogen for the complete Abreaktion of nitro groups. to Creation of Figure 5 (or similar diagrams) required substance data can be taken, for example, the familiar to the expert database DIPPR. At ATadiabat> +3 K, fresh catalyst is added to ensure that the adiabatically operated reaction space is not overloaded. Example 3 (according to the invention)

In the setup of Example 1, 15 grams of catalyst, suspended in water, are weighed and the reaction is begun. Each time ATadiabat exceeds 1K, 3g of catalyst is added. The reaction product exiting the adiabatic reaction space (stream 4) is regularly analyzed by gas chromatography; DNT, nitrotoluidines and nitroso compounds are not found.

Claims

Claims:

1. A process for the preparation of aromatic amines of the formula

in which R 1 and R 2 independently of one another are hydrogen, methyl or ethyl, where R 1 can additionally denote NH ₂ , by hydrogenation in the presence of a catalyst of nitroaromatics of the formula

in which R 2 and R 3 independently of one another denote hydrogen, methyl or ethyl, where R 3 may additionally denote NO 2, in the liquid phase in at least two series-connected reaction chambers arranged in one reactor or in several reactors, at least one reaction space being isothermal and at least the reaction space downstream thereof is operated adiabatically.

2. The method of claim 1, wherein the reaction course of the hydrogenation is monitored by controlling a characteristic of the performed in at least one of the adiabatically operated reaction chamber part of the characteristic hydrogenation and on reaching or exceeding a critical value of this characteristic at least one process parameter is changed so that this parameter again falls below the critical value, wherein the appropriate characteristic is selected from the group consisting of color, temperature, concentration of compounds containing nitro and nitroso groups.

3. The method of claim 2, wherein the suitable characteristic is the temperature measured in at least one of the adiabatically operated reaction spaces or in the product outlet from at least one of the adiabatically operated reaction chambers tadiabat.

4. The method of claim 3, wherein the critical value of the characteristic Tadiabat is between 200 ° C and 250 ° C.

5. The method of claim 2, wherein the concentration of nitro and nitroso-containing compounds is determined by chemical or spectroscopic analysis.

6. The method of claim 2, wherein the suitable characteristic variable is the temperature difference ATadiabat = Tadiabat-T _isoth erm between at least one of the adiabatically operated reaction spaces and the latter each isothermal reaction space, and

Tadiabat in the product outlet from the respective adiabatically operated reaction space or in the respective adiabatically operated reaction space and

Tisotherm be measured in the respective preceding isothermally operated reaction space or in the entry into the respective adiabatically operated reaction space.

7. The method of claim 6, wherein the critical value of the characteristic ATadiabat (ATadiabat, crit.) Is between -10 K and +8 K.

8. The method according to any one of claims 2 to 7, wherein the change of the at least one process parameter is selected from the possibilities: a) supply of fresh catalyst; b) increasing the recycled amount of used catalyst; c) Gradually reducing the amount of fresh nitroaromatic feed; d) increasing the pressure in at least one of the reaction spaces; e) increasing the temperature in at least one of the reaction spaces.

9. The method according to any one of claims 1 to 8, wherein in all reaction chambers in each case temperatures of 50 ° C to 250 ° C and absolute pressures of 6 bar to 101 bar are maintained.

10. The process according to claim 9, wherein the ratio of the pressure in any adiabatically operated reaction space to the pressure in the respectively preceding isothermally operated reaction space is greater than 0.5. Method according to one of claims 1 to 10, wherein dinitrotoluene (in formula II: R2 = methyl and R3 = N0 ₂ ) to toluene diamine (in formula I: Rl = NH ₂ and R2 = methyl) is hydrogenated.

A method according to any one of claims 1 to 11, wherein between 2 and 10 reaction spaces are connected in series.

Method according to one of claims 1 to 12, wherein the first reaction space in the direction of flow of the nitro aromatic isothermal and the last adiabatic operated.